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Case report
DOI: 10.1016/j.redare.2020.04.008
Anesthetic management of Kearns–Sayre syndrome. Case report
Tratamiento anestésico en el síndrome de Kearns–Sayre. Descripción de un caso
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J. Talaván Sernaa,
Corresponding author
jutaser@alumni.uv.es

Corresponding author.
, L. Belmonte Bayoa, E. Gutiérrez Ruedaa, S. Rodríguez Martínezb
a Servicio de Anestesiología y Reanimación, Hospital Obispo Polanco, Teruel, Spain
b Servicio de Urgencias, Hospital Obispo Polanco, Teruel, Spain
Received 21 February 2020. Accepted 17 April 2020
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Abstract

Kearns–Sayre syndrome is a mitochondrial myopathy characterised by ophthalmoplegia, pigmentary retinopathy and cardiac conduction abnormalities. This article describes the clinical management of a 50-year-old patient with Kearns–Sayre syndrome who underwent subarachnoid anaesthesia for a traumatic femoral fracture surgery.

Keywords:
Kearns–Sayre syndrome
Mitochondrial disease
Spinal anesthesia
Case management
Resumen

El síndrome de Kearns-Sayre constituye una miopatía mitocondrial que cursa con oftalmoplejia, retinopatía pigmentaria y alteraciones de la conducción cardiaca. Presentamos el caso de un paciente de 50 años de edad con síndrome de Kearns-Sayre intervenido de una fractura de fémur con anestesia subaracnoidea.

Palabras clave:
Kearns-Sayre síndrome
Enfermedad mitocondrial
Anestesia espinal
Tratamiento

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